SureForm 45, SureForm 45 Reloads

System, Surgical, Computer Controlled Instrument

Intuitive Surgical

The following data is part of a premarket notification filed by Intuitive Surgical with the FDA for Sureform 45, Sureform 45 Reloads.

Pre-market Notification Details

Device IDK183224
510k NumberK183224
Device Name:SureForm 45, SureForm 45 Reloads
ClassificationSystem, Surgical, Computer Controlled Instrument
Applicant Intuitive Surgical 1266 Kifer Road Sunnyvale,  CA  94086
ContactNadine Nasr
CorrespondentNadine Nasr
Intuitive Surgical 1266 Kifer Road Sunnyvale,  CA  94086
Product CodeNAY  
CFR Regulation Number876.1500 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2018-11-20
Decision Date2019-01-18
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
10886874117580 K183224 000
10886874117122 K183224 000
10886874117115 K183224 000
10886874117092 K183224 000
10886874117085 K183224 000

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